Source: INFERRED ×
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C0202115
Disease: Lactic acid measurement
Lactic acid measurement 		0 2 0 0 1 1.4E-02
CUI: C0523573
Disease: Citrulline measurement
Citrulline measurement 		0 1 0 0 1 1.5E-02
CUI: C0523920
Disease: Threonine measurement
Threonine measurement 		0 5 0 0 1 1.4E-02
CUI: C0730345
Disease: Microalbuminuria
Microalbuminuria 		0 32 0 0 1 1.0E-02
CUI: C2239222
Disease: Vascular Endothelial Growth Factor Measurement
Vascular Endothelial Growth Factor Measurement 		0 46 0 0 1 8.8E-03
CUI: C0220710
Disease: Medium-chain acyl-coenzyme A dehydrogenase deficiency
Medium-chain acyl-coenzyme A dehydrogenase deficiency 		1 0 1 3.1E-02 0 0
CUI: C0272339
Disease: Prekallikrein deficiency
Prekallikrein deficiency 		1 0 1 3.1E-02 0 0
CUI: C0472803
Disease: Hypodysfibrinogenemia
Hypodysfibrinogenemia 		1 0 1 3.1E-02 0 0
CUI: C1291463
Disease: Deficiency of phosphoserine phosphatase
Deficiency of phosphoserine phosphatase 		1 0 1 3.1E-02 0 0
CUI: C1706410
Disease: Atopic IgE-mediated allergic disorder
Atopic IgE-mediated allergic disorder 		1 0 1 3.1E-02 0 0
CUI: C1850533
Disease: Yellow subcutaneous tissue covered by thin, scaly skin
Yellow subcutaneous tissue covered by thin, scaly skin 		1 0 1 3.1E-02 0 0
CUI: C1858493
Disease: FEBRILE CONVULSIONS, FAMILIAL, 4
FEBRILE CONVULSIONS, FAMILIAL, 4 		1 0 1 3.1E-02 0 0
CUI: C1860081
Disease: Medium chain dicarboxylic aciduria
Medium chain dicarboxylic aciduria 		1 0 1 3.1E-02 0 0
CUI: C1866174
Disease: Phosphoglycerate Dehydrogenase Deficiency
Phosphoglycerate Dehydrogenase Deficiency 		1 0 1 3.1E-02 0 0
CUI: C3541908
Disease: Sperm Motility Measurement
Sperm Motility Measurement 		1 0 1 3.1E-02 0 0
CUI: C3552528
Disease: Generalized ichthyosis
Generalized ichthyosis 		1 0 1 3.1E-02 0 0
CUI: C3714958
Disease: PULMONARY HYPERTENSION, NEONATAL, SUSCEPTIBILITY TO
PULMONARY HYPERTENSION, NEONATAL, SUSCEPTIBILITY TO 		1 0 1 3.1E-02 0 0
CUI: C3715155
Disease: AMYOTROPHIC LATERAL SCLEROSIS 19
AMYOTROPHIC LATERAL SCLEROSIS 19 		1 0 1 3.1E-02 0 0
CUI: C4016097
Disease: FIBRINOGEN MILANO XII, DIGENIC PHENOTYPE
FIBRINOGEN MILANO XII, DIGENIC PHENOTYPE 		1 0 1 3.1E-02 0 0
CUI: C4022414
Disease: Elevated urinary 3-hydroxybutyric acid
Elevated urinary 3-hydroxybutyric acid 		1 0 1 3.1E-02 0 0
CUI: C4023465
Disease: EEG with occipital slowing
EEG with occipital slowing 		1 0 1 3.1E-02 0 0
CUI: C4082171
Disease: Hyperammonemia Due to Carbamoyl Phosphate Synthetase 1 Deficiency
Hyperammonemia Due to Carbamoyl Phosphate Synthetase 1 Deficiency 		1 0 1 3.1E-02 0 0
CUI: C4225203
Disease: HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2
HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 2 		1 0 1 3.1E-02 0 0
CUI: C4280778
Disease: Modic type vertebral endplate changes
Modic type vertebral endplate changes 		1 0 1 3.1E-02 0 0
CUI: C4551478
Disease: NEU-LAXOVA SYNDROME 1
NEU-LAXOVA SYNDROME 1 		1 0 1 3.1E-02 0 0